510(k) K191339 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Zavation eZspand Interbody System
| Applicant | Zavation Medical Products, LLC, Flowood MS, US |
| Decision | Substantially Equivalent, Aug 19, 2019 |
| Received | May 20, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191339
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.